GlyCosmos Portal

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Displaying entries **3326 - 3350** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▲	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P09622	Dihydrolipoyl dehydrogenase, mitochondrial	DLD GCSL LAD PHE3	Homo sapiens (human)	2	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Friedreich ataxia Glanzmann's thrombasthenia Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute monocytic leukemia acute myocardial infarction adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma adult fibrosarcoma alexia alternating hemiplegia of childhood amyotrophic lateral sclerosis antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autonomic neuropathy bacterial sepsis benign mesothelioma brain disease brain infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia choriocarcinoma chromophobe renal cell carcinoma chronic monocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communication disorder congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc congenital disorder of glycosylation congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma cutaneous mastocytosis dementia depressive disorder diabetes mellitus diabetic ketoacidosis diffuse cutaneous mastocytosis disease of metabolism dyslexia dysthymic disorder dystonia embryoma endomyocardial fibrosis epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypertrophic cardiomyopathy fibrosarcoma follicular adenoma fragile X syndrome frontotemporal dementia giant cell glioblastoma glioblastoma granular cell carcinoma gray platelet syndrome hepatic coma hepatic encephalopathy hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypertensive retinopathy hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermittent claudication islet cell tumor lactic acidosis language disorder large intestine cancer learning disability leukemia leukocyte adhesion deficiency 2 leukocyte adhesion deficiency 3 leukocyte adhesion deficiency lissencephaly liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lymphoid leukemia major depressive disorder malignant mesothelioma maple syrup urine disease mastocytosis melancholic depression methemoglobinemia microcephaly microcystic adenoma monocytic leukemia multiple myeloma multiple sclerosis myeloid leukemia myocardial infarction nervous system disease neuroblastoma neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma periodontitis peripheral vascular disease placenta cancer platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 posterior myocardial infarction primary immunodeficiency disease progressive muscular atrophy prostate cancer prostate carcinoma protein C deficiency protein S deficiency pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency qualitative platelet defect renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia short chain acyl-CoA dehydrogenase deficiency silent myocardial infarction stomach cancer stomach carcinoma stuttering sulfhemoglobinemia thrombophilia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urea cycle disorder urticaria pigmentosa varicose veins vascular disease viral infectious disease visual epilepsy
Q12959	Disks large homolog 1	DLG1	Homo sapiens (human)	5	3
Q15700	Disks large homolog 2	DLG2	Homo sapiens (human)	0	1
P78352	Disks large homolog 4	DLG4 PSD95	Homo sapiens (human)	0	1
Q8TDM6	Disks large homolog 5	DLG5 KIAA0583 PDLG	Homo sapiens (human)	9	2
O14490	Disks large-associated protein 1	DLGAP1 DAP1 GKAP	Homo sapiens (human)	4	1
Q9P1A6	Disks large-associated protein 2	DLGAP2 C8orf68 DAP2 ERICH1-AS1	Homo sapiens (human)	3	3
Q9Y2H0	Disks large-associated protein 4	DLGAP4 DAP4 KIAA0964 SAPAP4	Homo sapiens (human)	2	2
Q15398	Disks large-associated protein 5	DLGAP5 DLG7 KIAA0008	Homo sapiens (human)	2	1
P80370	Protein delta homolog 1	DLK1 DLK	Homo sapiens (human)	15	3
Q6UY11	Protein delta homolog 2	DLK2 EGFL9	Homo sapiens (human)	1	0
O00548	Delta-like protein 1	DLL1	Homo sapiens (human)	2	1
Q9NR61	Delta-like protein 4	DLL4	Homo sapiens (human)	4	0
P36957	Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial	DLST DLTS	Homo sapiens (human)	2	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Joubert syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Wernicke-Korsakoff syndrome adrenal gland cancer amnestic disorder aniridia cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome duodenum cancer glomerulonephritis heart cancer hydranencephaly hypercalcemia hypertensive retinopathy kidney disease lissencephaly nephritis nephrocalcinosis neurodegenerative disease panic disorder papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary biliary cholangitis prostate cancer prostate carcinoma proteinuria renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid renal cell carcinoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly small intestine cancer syndromic X-linked intellectual disability Najm type
P56177	Homeobox protein DLX-1	DLX1	Homo sapiens (human)	0	1
Q96GE9	Distal membrane-arm assembly complex protein 1	DMAC1 C9orf123 TMEM261	Homo sapiens (human)	0	1
Q9NW81	Distal membrane-arm assembly complex protein 2	DMAC2 ATP5SL	Homo sapiens (human)	0	1
Q9NPF5	DNA methyltransferase 1-associated protein 1	DMAP1 KIAA1425	Homo sapiens (human)	4	2
Q9UGM3	Deleted in malignant brain tumors 1 protein	DMBT1 GP340	Homo sapiens (human)	26	1
Q8NFW5	Diencephalon/mesencephalon homeobox protein 1	DMBX1 MBX OTX3 PAXB	Homo sapiens (human)	1	1
P11532	Dystrophin	DMD	Homo sapiens (human)	6	3	Duchenne muscular dystrophy
Q6E0U4	Dermokine	DMKN	Homo sapiens (human)	2	1
Q13316	Dentin matrix acidic phosphoprotein 1	DMP1	Homo sapiens (human)	8	0
Q9Y5R5	Doublesex- and mab-3-related transcription factor 2	DMRT2 DSXL2	Homo sapiens (human)	0	1
Q9NQL9	Doublesex- and mab-3-related transcription factor 3	DMRT3 DMRTA3	Homo sapiens (human)	1	1

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